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Flagellar, Cellular and Organismal Polarity in Volvox Carteri
SUNY Geneseo KnightScholar Biology Faculty/Staff Works Department of Biology 1993 Flagellar, cellular and organismal polarity in Volvox carteri Harold J. Hoops SUNY Geneseo Follow this and additional works at: https://knightscholar.geneseo.edu/biology Recommended Citation Hoops H.J. (1993) Flagellar, cellular and organismal polarity in Volvox carteri. Journal of Cell Science 104: 105-117. doi: This Article is brought to you for free and open access by the Department of Biology at KnightScholar. It has been accepted for inclusion in Biology Faculty/Staff Works by an authorized administrator of KnightScholar. For more information, please contact [email protected]. Journal of Cell Science 104, 105-117 (1993) 105 Printed in Great Britain © The Company of Biologists Limited 1993 Flagellar, cellular and organismal polarity in Volvox carteri Harold J. Hoops Department of Biology, 1 Circle Drive, SUNY-Genesco, Genesco, NY 14454, USA SUMMARY It has previously been shown that the flagellar appara- reorientation of flagellar apparatus components. This tus of the mature Volvox carteri somatic cell lacks the reorientation also results in the movement of the eye- 180˚ rotational symmetry typical of most unicellular spot from a position nearer one of the flagellar bases to green algae. This asymmetry has been postulated to be a position approximately equidistant between them. By the result of rotation of each half of the flagellar appa- analogy to Chlamydomonas, the anti side of the V. car - ratus. Here it is shown that V. carteri axonemes contain teri somatic cell faces the spheroid anterior, the syn side polarity markers that are similar to those found in faces the spheroid posterior. -
Algal Sex Determination and the Evolution of Anisogamy James Umen, Susana Coelho
Algal Sex Determination and the Evolution of Anisogamy James Umen, Susana Coelho To cite this version: James Umen, Susana Coelho. Algal Sex Determination and the Evolution of Anisogamy. Annual Review of Microbiology, Annual Reviews, 2019, 73 (1), 10.1146/annurev-micro-020518-120011. hal- 02187088 HAL Id: hal-02187088 https://hal.sorbonne-universite.fr/hal-02187088 Submitted on 17 Jul 2019 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. Annu. Rev. Microbiol. 2019. 73:X–X https://doi.org/10.1146/annurev-micro-020518-120011 Copyright © 2019 by Annual Reviews. All rights reserved Umen • Coelho www.annualreviews.org • Algal Sexes and Mating Systems Algal Sex Determination and the Evolution of Anisogamy James Umen1 and Susana Coelho2 1Donald Danforth Plant Science Center, St. Louis, Missouri 63132, USA; email: [email protected] 2Sorbonne Université, UPMC Université Paris 06, CNRS, Algal Genetics Group, UMR 8227, Integrative Biology of Marine Models, Station Biologique de Roscoff, CS 90074, F-29688, Roscoff, France [**AU: Please write the entire affiliation in French or write it all in English, rather than a combination of English and French**] ; email: [email protected] Abstract Algae are photosynthetic eukaryotes whose taxonomic breadth covers a range of life histories, degrees of cellular and developmental complexity, and diverse patterns of sexual reproduction. -
Detergent-Extracted Volvox Model Exhibits an Anterior–Posterior Gradient in Flagellar Ca2+ Sensitivity
Detergent-extracted Volvox model exhibits an PNAS PLUS + anterior–posterior gradient in flagellar Ca2 sensitivity Noriko Uekia and Ken-ichi Wakabayashia,1 aLaboratory for Chemistry and Life Science, Institute of Innovative Research, Tokyo Institute of Technology, Yokohama-shi, Kanagawa 226-8503, Japan Edited by Krishna K. Niyogi, Howard Hughes Medical Institute, University of California, Berkeley, CA, and approved December 8, 2017 (received for review September 1, 2017) Volvox rousseletii is a multicellular spheroidal green alga contain- suggested by studies using demembranated and reactivated cells ing ∼5,000 cells, each equipped with two flagella (cilia). This or- and flagella (5, 6). ganism shows striking photobehavior without any known Multicellular spheroidal species of Volvocales, including Volvox intercellular communication. To help understand how the behav- species, have often been regarded as colonial Chlamydomonas. ior of flagella is regulated, we developed a method to extract the However, alignment of Chlamydomonas cells on the surface of a whole organism with detergent and reactivate its flagellar motil- spheroid, with each cell displaying breaststroke-like flagellar ity. Upon addition of ATP, demembranated flagella (axonemes) in beating, would result in spheroids unable to swim in one direction. the spheroids actively beat and the spheroids swam as if they Unlike a C. reinhardtii cell, each cell in a Volvox spheroid has two + were alive. Under Ca2 -free conditions, the axonemes assumed flagella beating in the same direction. A Volvox spheroid has an planar and asymmetrical waveforms and beat toward the poste- anterior–posterior (A–P) axis, and its ∼10,000 flagella beat toward rior pole, as do live spheroids in the absence of light stimulation. -
Lateral Gene Transfer of Anion-Conducting Channelrhodopsins Between Green Algae and Giant Viruses
bioRxiv preprint doi: https://doi.org/10.1101/2020.04.15.042127; this version posted April 23, 2020. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC-ND 4.0 International license. 1 5 Lateral gene transfer of anion-conducting channelrhodopsins between green algae and giant viruses Andrey Rozenberg 1,5, Johannes Oppermann 2,5, Jonas Wietek 2,3, Rodrigo Gaston Fernandez Lahore 2, Ruth-Anne Sandaa 4, Gunnar Bratbak 4, Peter Hegemann 2,6, and Oded 10 Béjà 1,6 1Faculty of Biology, Technion - Israel Institute of Technology, Haifa 32000, Israel. 2Institute for Biology, Experimental Biophysics, Humboldt-Universität zu Berlin, Invalidenstraße 42, Berlin 10115, Germany. 3Present address: Department of Neurobiology, Weizmann 15 Institute of Science, Rehovot 7610001, Israel. 4Department of Biological Sciences, University of Bergen, N-5020 Bergen, Norway. 5These authors contributed equally: Andrey Rozenberg, Johannes Oppermann. 6These authors jointly supervised this work: Peter Hegemann, Oded Béjà. e-mail: [email protected] ; [email protected] 20 ABSTRACT Channelrhodopsins (ChRs) are algal light-gated ion channels widely used as optogenetic tools for manipulating neuronal activity 1,2. Four ChR families are currently known. Green algal 3–5 and cryptophyte 6 cation-conducting ChRs (CCRs), cryptophyte anion-conducting ChRs (ACRs) 7, and the MerMAID ChRs 8. Here we 25 report the discovery of a new family of phylogenetically distinct ChRs encoded by marine giant viruses and acquired from their unicellular green algal prasinophyte hosts. -
Some Algae in Lakes Hume and Mulwala Victoria
S0£.1E ALGAE IN LAKES HUHE AND HUT~WALA (1974) VICTORIA ·By KANJANA VIYAKORNVILAS B.Sc. (Tas.) A Thesis submitted in partial fulfilment of the requirements for the Degree of Bachelor of Science with Honours at the University of Tasmania. I hereby declare that this thesis contains no material which has been accepted for the award of any other degree in any university and that, to the best of my kno\vledge, the thesis contains no copy or paraphase of material previously published or written by another person, except when due reference is made in the text. -•ACKNO\'/I,EDGEl·fEN a---1:es I wish to express my sincere thanks to Dr .. P@A~Tyler, my supervisor, for his helpful advice and criticism .. Hr .. R.L.Croome for collecting all the samples .. Mrs .. R .. ivickham for her technical advice. All members of the Botany Dept .. for their assistance at various times of the year .. K.. Viyalwrnvilas, Botany Dept .. , University of Tasmania, November 1974 .. CONTENTS·-«"· .... Page Summary 1 Introduction 2 Materials and Method 2 Results 4 Systematic account 13 Division Chlorophyta-Class Chlorophyceae 13 Chrysophyta-Class Chrysophyceae 65 Class Bacteriophyceae 68 II Euglenophyta-Class Euglenophyceae 79 It Pyrrhophyta-Class Dinophyceae 86 Cyanophyta -Class Cyanophyceae 87 Discussion The trophic status of Lakes Hume and Hulwala 93 Geographical distribution of desmids seen 95 Plates 1-14 and Explana·tion of plates 96 Literature cited 116 l SUNMARY Lakes IIume and Hulwala have very similar plankton communi ties in which N.e.l.?.si,r.a .Ei.X:~£U~ Ralfs is dominant .. The species composition and the plankton quotients show the t\<IO lakes are mesotrophic.Host of the algae seen are well-lmown and widespread . -
Phylogenetic Analysis and Substitution Rate Estimation of Colonial Volvocine Algae Based on Mitochondrial Genomes
G C A T T A C G G C A T genes Article Phylogenetic Analysis and Substitution Rate Estimation of Colonial Volvocine Algae Based on Mitochondrial Genomes Yuxin Hu 1,2, Weiyue Xing 1,2, Zhengyu Hu 3 and Guoxiang Liu 1,* 1 Key Laboratory of Algal Biology, Institute of Hydrobiology, Chinese Academy of Sciences, Wuhan 430072, China; [email protected] (Y.H.); [email protected] (W.X.) 2 School of Life Sciences, University of Chinese Academy of Sciences, Beijing 100049, China 3 State Key Laboratory of Freshwater Ecology and Biotechnology, Institute of Hydrobiology, Chinese Academy of Sciences, Wuhan 430072, China; [email protected] * Correspondence: [email protected]; Tel.: +86-027-6878-0576 Received: 11 December 2019; Accepted: 15 January 2020; Published: 20 January 2020 Abstract: We sequenced the mitochondrial genome of six colonial volvocine algae, namely: Pandorina morum, Pandorina colemaniae, Volvulina compacta, Colemanosphaera angeleri, Colemanosphaera charkowiensi, and Yamagishiella unicocca. Previous studies have typically reconstructed the phylogenetic relationship between colonial volvocine algae based on chloroplast or nuclear genes. Here, we explore the validity of phylogenetic analysis based on mitochondrial protein-coding genes. Wefound phylogenetic incongruence of the genera Yamagishiella and Colemanosphaera. In Yamagishiella, the stochastic error and linkage group formed by the mitochondrial protein-coding genes prevent phylogenetic analyses from reflecting the true relationship. In Colemanosphaera, a different reconstruction approach revealed a different phylogenetic relationship. This incongruence may be because of the influence of biological factors, such as incomplete lineage sorting or horizontal gene transfer. We also analyzed the substitution rates in the mitochondrial and chloroplast genomes between colonial volvocine algae. -
Evolution Der Algen Und Plastiden (T
Georg-August-Universität Göttingen Vorlesung 63052 Biodiversität: Evolution der Algen EvolutionEvolution derder AlgenAlgen undund PlastidenPlastiden Teil 5: Viridiplantae Thomas Friedl Abteilung Experimentelle Phykologie undund Sammlung von Algenkulturen Albrecht-von-Haller-Institut für Pflanzenwissenschaften www.epsag.uni-goettingen.de Biodiversität: Evolution der Algen WS 2007/8 Mi 12:15 - 13:00 im Seminarraum 1.213 oder kleinen Hörsaal Evolution der Algen und Plastiden (T. Friedl) 17.10. Einführung, Übersicht über die Algen, Vorstellung der Abteilung EPSAG 24.10. Cyanobakterien 31.10. - Besichtigung der Abteilung und SAG (I. Lang) - 07.11. -- 14.11. Primäre Endosymbiose 21.11. Glaucophyta, Rotalgen 28.11. Grünalgen und Entstehung der Landpflanzen 05.12. Sekundäre Endosymbiose, Cryptophyta, Chlorarachniophyta 12.12. Stramenopiles + Haptophyta = "Chromista"? 19.12. Alveolates,Euglenozoa, Abschlußbetrachtung 09.01. Imke Lang: Cryokonservierung 16.01. Imke Lang: Anwendung von Algen in der Biotechnologie 23.01 Kathrin Mohr: Erfassen von Algenbiodiversität mit molekularen Methoden. I 30.01 Kathrin Mohr: Erfassen von Algenbiodiversität mit molekularen Methoden. II Benutzername: evolution Passwort: ers01ter www.epsag.uni-goettingen.de Primary endosymbiosis Secondary endosymbiosis Tertiary endosymbiosis Cyanobacterium Ciliates primary host Rhodophyta Sporozoa Glaucophyta Chlorophyta secondary host peridinin-containing Dinoflagellates Heterokontophyta, secondary host Haptophyta tertiary host fucoxanthin-containing Dinoflagellates Oomycetes heteroloboseid -
New and Rare Species of Volvocaceae (Chlorophyta) in the Polish Phycoflora
Acta Societatis Botanicorum Poloniae Journal homepage: pbsociety.org.pl/journals/index.php/asbp ORIGINAL RESEARCH PAPER Received: 2013.06.25 Accepted: 2013.12.15 Published electronically: 2013.12.20 Acta Soc Bot Pol 82(4):259–266 DOI: 10.5586/asbp.2013.038 New and rare species of Volvocaceae (Chlorophyta) in the Polish phycoflora Ewa Anna Dembowska* Department of Hydrobiology, Nicolaus Copernicus University, Lwowska 1, 87-100 Toruń, Poland Abstract Seven species of Volvocaceae were recorded in the lower Vistula River and its oxbow lakes, including Pleodorina californica for the first time in Poland. Three species – Eudorina cylindrica, E. illinoisensis and E. unicocca – were found in the Polish Vistula River in the 1960s and 1970s, as well as at present. They are rare species in the Polish aquatic ecosystems. Three species are com- mon both in the oxbow lakes and in the Vistula River: Eudorina elegans, Pandorina morum and Volvox aureus. New and rare Volvocaceae species were described in terms of morphology and ecology; also photographic documentation (light microscope microphotographs) was completed. Keywords: Pleodorina, Pandorina, Eudorina, biodiversity, phytoplankton, oxbow lake, lower Vistula Introduction Green algae from the family of Volvocaceae are frequently encountered in eutrophic waters. All species from this family The family of Volvocaceae (Chlorophyta, Volvocales) com- live in fresh waters: lakes, ponds, rivers, and even puddles. prises 7 genera: Eudorina, Pandorina, Platydorina, Pleodorina, Coleman [1] reports that out of ca. 200 colonial Volvocaceae Volvox, Volvulina and Yamagishiella [1]. The genera Astre- in culture collections, ~1/3 came from puddles, ~1/3 – from phomene and Gonium were excluded from Volvocaceae and they lakes and rice fields, and ~1/3 – from zygotes in soil samples form new families: Goniaceae – based on the ultrastructure of from watersides. -
Evolution of Cytokinesis-Related Protein Localization During The
Arakaki et al. BMC Evolutionary Biology (2017) 17:243 DOI 10.1186/s12862-017-1091-z RESEARCH ARTICLE Open Access Evolution of cytokinesis-related protein localization during the emergence of multicellularity in volvocine green algae Yoko Arakaki1, Takayuki Fujiwara2, Hiroko Kawai-Toyooka1, Kaoru Kawafune1,3, Jonathan Featherston4,5, Pierre M. Durand4,6, Shin-ya Miyagishima2 and Hisayoshi Nozaki1* Abstract Background: The volvocine lineage, containing unicellular Chlamydomonas reinhardtii and differentiated multicellular Volvox carteri, is a powerful model for comparative studies aiming at understanding emergence of multicellularity. Tetrabaena socialis is the simplest multicellular volvocine alga and belongs to the family Tetrabaenaceae that is sister to more complex multicellular volvocine families, Goniaceae and Volvocaceae. Thus, T. socialis is a key species to elucidate the initial steps in the evolution of multicellularity. In the asexual life cycle of C. reinhardtii and multicellular volvocine species, reproductive cells form daughter cells/colonies by multiple fission. In embryogenesis of the multicellular species, daughter protoplasts are connected to one another by cytoplasmic bridges formed by incomplete cytokinesis during multiple fission. These bridges are important for arranging the daughter protoplasts in appropriate positions such that species-specific integrated multicellular individuals are shaped. Detailed comparative studies of cytokinesis between unicellular and simple multicellular volvocine species will help to elucidate the emergence of multicellularity from the unicellular ancestor. However, the cytokinesis-related genes between closely related unicellular and multicellular species have not been subjected to a comparative analysis. Results: Here we focused on dynamin-related protein 1 (DRP1), which is known for its role in cytokinesis in land plants. Immunofluorescence microscopy using an antibody against T. -
Green Algae and the Origins of Multicellularity in the Plant Kingdom
Downloaded from http://cshperspectives.cshlp.org/ on October 8, 2021 - Published by Cold Spring Harbor Laboratory Press Green Algae and the Origins of Multicellularity in the Plant Kingdom James G. Umen Donald Danforth Plant Science Center, St. Louis, Missouri 63132 Correspondence: [email protected] The green lineage of chlorophyte algae and streptophytes form a large and diverse clade with multiple independent transitions to produce multicellular and/or macroscopically complex organization. In this review, I focus on two of the best-studied multicellular groups of green algae: charophytes and volvocines. Charophyte algae are the closest relatives of land plants and encompass the transition from unicellularity to simple multicellularity. Many of the innovations present in land plants have their roots in the cell and developmental biology of charophyte algae. Volvocine algae evolved an independent route to multicellularity that is captured by a graded series of increasing cell-type specialization and developmental com- plexity. The study of volvocine algae has provided unprecedented insights into the innova- tions required to achieve multicellularity. he transition from unicellular to multicellu- and rotifers that are limited by prey size (Bell Tlar organization is considered one of the ma- 1985; Boraas et al. 1998). Reciprocally, increased jor innovations in eukaryotic evolution (Szath- size might also entail advantages in capturing ma´ry and Maynard-Smith 1995). Multicellular more or larger prey. organization can be advantageous for several There is some debate about how easy or reasons. Foremost among these is the potential difficult it has been for unicellular organisms for cell-type specialization that enables more to evolve multicellularity (Grosberg and Strath- efficient use of scarce resources and can open mann 2007). -
The Flagellar Photoresponse in Volvox Species (Volvocaceae, Chlorophyceae)1
J. Phycol. 47, ***–*** (2011Diana) Ó 2011Diana Phycological Society of America DOI: 10.1111/j.1529-8817.2011.00983.x NOTE THE FLAGELLAR PHOTORESPONSE IN VOLVOX SPECIES (VOLVOCACEAE, CHLOROPHYCEAE)1 Cristian A. Solari2 CONICET, Departamento de Biodiversidad y Biologı´a Experimental (FCEyN), Laboratorio de Biologı´a Comparada de Protistas, Universidad de Buenos Aires, Buenos Aires C1428EHA, Argentina Knut Drescher and Raymond E. Goldstein Department of Applied Mathematics and Theoretical Physics, University of Cambridge, Cambridge CB3 0WA, UK Steering their swimming direction toward the light specialization, each of the Chlamydomonas-like somatic is crucial for the viability of Volvox colonies, the lar- cells is positioned at the surface of the extracellular ger members of the volvocine algae. While it is matrix, with its two flagella oriented outward, while known that this phototactic steering is achieved by a the germ cells grow inside the colony. Volvox species difference in behavior of the flagella on the illumi- with germ-soma separation have evolved several times nated and shaded sides, conflicting reports suggest independently from quite different colonial ancestors that this asymmetry arises either from a change in with no cellular differentiation (Coleman 1999, No- beating direction or a change in beating frequency. zaki et al. 1999, 2006, Nozaki 2003, Herron and Mi- Here, we report direct observations of the flagellar chod 2008). These species with different phyletic behavior of various Volvox species with different phy- origin have been classified within the volvocine algae letic origin in response to light intensity changes and into different sections ⁄ groups (Smith 1944, Nozaki thereby resolve this controversy: Volvox barberi W. -
Green Microalga Trebouxia Sp. Produces Strigolactone
bioRxiv preprint doi: https://doi.org/10.1101/195883; this version posted September 29, 2017. The copyright holder for this preprint (which was not certified by peer review) is the author/funder. All rights reserved. No reuse allowed without permission. 1 1 Green microalga Trebouxia sp. produces strigolactone- 2 related compounds 3 4 Smýkalová I.1, Ludvíková M.1, Ondráčková E.1, Klejdus B.2, Bonhomme S.3, Kronusová O.4, 5 Soukup A.5, Rozmoš M.6, Guzow-Krzemińska B.7, Matúšová R.8 6 7 1 Agritec Plant Research Ltd., Zemědělská 16, Šumperk, 787 01, Czech Republic; 8 2 Department of Chemistry and Biochemistry, Mendel University in Brno, Zemědělská 1, 9 Brno, 613 00 Brno, Czech Republic; 10 3 Institut Jean-Pierre Bourgin, INRA, AgroParisTech, CNRS, Université Paris-Saclay, Route 11 de St-Cyr 10, 780 26 Versailles Cedex, France. 12 4 Ecofuel Laboratories Ltd., Ocelářská 9, 190 02 Prague, Czech Republic; 13 5 Department of Experimental Plant Biology, Faculty of Science Charles University in 14 Prague, Viničná 5, 128 44 Prague 2, Czech Republic; 15 6 Institute of Experimental Biology, Faculty of Plant Science, Masaryk University, Kotlářská 16 267/2 , Brno, 611 37, Czech Republic; 17 7 Department of Plant Taxonomy and Narture Conservation, Faculty of Biology, University 18 of Gdańsk, Wita Stwosza 59, 80-308 Gdańsk, Poland; 19 8 Plant Science and Biodiversity Center SAS, Institute of Plant Genetics and Biotechnology, 20 Akademicka 2, PO Box 39A, 95007 Nitra, Slovak Republic; 21 22 Corresponding authors: [email protected]; [email protected] 23 Running title 24 Production of SLs in microalga 25 Highlight 26 In lichenized alga Trebouxia arboricola there are produced SLs-related compounds inducing 27 germination of parasitic weed Phelipanche aegyptiaca; T.